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Jobs at Iqvia in United Kingdom

Associate Director - Clinical Leads

QUK IQVIA Ltd.

Reading
On-site
GBP 125,000 - 150,000
30+ days ago
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Phlebotomist - Chichester/Horsham

IQVIA Digital, Inc. (USB1)

England
On-site
GBP 60,000 - 80,000
30+ days ago

Territory Business Manager

IQVIA

Reading
On-site
GBP 125,000 - 150,000
30+ days ago

National Key Account Manager

IQVIA

Matlock
Remote
GBP 60,000 - 80,000
30+ days ago

Medical Sales Representative

IQVIA

Penryn
On-site
GBP 30,000 - 45,000
30+ days ago
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Territory Business Manager

IQVIA Digital, Inc. (USB1)

Reading
On-site
GBP 125,000 - 150,000
30+ days ago

Medical Science Liaison, Oncology, UK, Ireland & Belgium

IQVIA, Inc.

Reading
On-site
GBP 60,000 - 80,000
30+ days ago

Medical Science Liaison, Oncology, UK, Ireland & Belgium

IQVIA Digital, Inc. (USB1)

Reading
On-site
GBP 60,000 - 80,000
30+ days ago
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Medical Sales Representative

IUK IQVIA IES UK Limited

Devon and Torbay
On-site
GBP 60,000 - 80,000
30+ days ago

Data Team Lead

QUK IQVIA Ltd.

Reading
On-site
GBP 100,000 - 125,000
30+ days ago

Medical Sales Representative

IUK IQVIA IES UK Limited

Cambridge
On-site
GBP 40,000 - 65,000
30+ days ago

Medical Sales Representative

IQVIA

Ipswich
On-site
GBP 40,000 - 55,000
30+ days ago

Key Account Manager

IQVIA

Belfast
On-site
GBP 35,000 - 45,000
30+ days ago

Key Account Manager

IQVIA

Derry/Londonderry
On-site
GBP 35,000 - 50,000
30+ days ago

Medical Sales Representative

IQVIA

Cambridge
On-site
GBP 30,000 - 45,000
30+ days ago

Medical Sales Representative

IQVIA

Colchester
On-site
GBP 60,000 - 80,000
30+ days ago

Key Account Manager

IUK IQVIA IES UK Limited

Belfast
On-site
GBP 30,000 - 45,000
30+ days ago

Strategic Director, Global Value and Access

IQVIA

London
On-site
GBP 70,000 - 120,000
30+ days ago

Senior Biostatistician - Oncology (FSP -Permanent Homebased)

IQVIA, Inc.

Reading
Remote
GBP 60,000 - 80,000
30+ days ago

Clinical Research Associate I

IQVIA, Inc.

Reading
On-site
GBP 35,000 - 50,000
30+ days ago

Clinical Research Associate II

IQVIA, Inc.

Reading
On-site
GBP 40,000 - 60,000
30+ days ago

Market Research Translation Project Manager

IQVIA Ltd. (GB80)

Reading
On-site
GBP 35,000 - 50,000
30+ days ago

Senior Biostatistician – Oncology (FSP -Permanent Homebased)

IQVIA

Reading
Remote
GBP 50,000 - 75,000
30+ days ago

Clinical Research Associate I

IQVIA

Reading
On-site
GBP 35,000 - 50,000
30+ days ago

Clinical Research Associate II

IQVIA Argentina

Reading
On-site
GBP 35,000 - 50,000
30+ days ago

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Associate Director - Clinical Leads
QUK IQVIA Ltd.
Reading
On-site
GBP 125,000 - 150,000
Full time
30+ days ago

Job summary

A global provider of clinical research services is seeking a seasoned leader to oversee Senior Global Trial Managers. The role involves ensuring project compliance, mentoring teams, and managing project risks, requiring a Bachelor's in life sciences and a robust background in clinical research with at least 10 years of experience, including leadership. This position is located in Reading, UK.

Qualifications

  • 10 years of clinical research experience including 6 years in leadership.
  • Proven ability to manage a team and work effectively with others.
  • Strong understanding of clinical trials and GCP/ICH guidelines.

Responsibilities

  • Provide oversight to Senior Global Trial Managers on project delivery.
  • Ensure compliance with regulatory and internal requirements.
  • Mentor team members and manage project risks.

Skills

Leadership
Clinical research experience
People Management
Collaboration
Communication
Organization
Results Oriented
IT Skills

Education

Bachelor's Degree in life sciences or related field

Tools

Microsoft Office
Job description

Job Overview
Provide oversight and leadership to Senior Global Trial managers (SGTMs) for project productivity, delivery and quality resulting in strong financial performance and customer satisfaction. Work with Clinical teams to focus on leveraging deep therapeutic expertise and IQVIA solutions to drive operational excellence and strategic leadership with our customers. Direct and manage an assigned team of clinical leads who lead or support studies or programs to make sure quality, time and budget deliverables are met to the Sponsor’s satisfaction and in accordance with Standard Operating Procedures (SOPs), policies and practices. Ensure Clinical leads are trained and individual development is aligned and in place to meet project and organizational needs. Attract, develop and retain talent.

Essential Functions
• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans). Ensure all Clinical Leads (CLs) obtain Fundamental Good Clinical Practices (GCP) accreditation during a two year cycle.
• Actively engage with SGTMs to review project performance and deliverables. Address performance issues and/or escalations by working to create action/recovery plans. Ensure compliance to the Clinical Leads (CL) metrics dashboard of all direct reports. Foster an environment where lessons learned are shared within the team.
• Ensure compliance on the overall Risk Management process including risks that are escalating into issues. Work with SGTMs on identification of risks that can lead to processes improvement/standardization across the organization.
• Ensure compliance to quality management processes that apply to all projects. Support quality initiatives and ensure quality metrics are met at all times.
• Mentor SGTMs to manage clinical aspects of Project Finances, Support to understand the scope of clinical delivery and create plans to deliver against this scope and to monitor and manage changes against baseline and identify additional service opportunities or out of scope work.

• Coach SGTMs to identify Out of Scope items, discuss impact and proactively suggest remediation plans when considering risks/delays and to determine appropriate action. Discuss and promote proactive identification of milestone risks by SGTMs
• Actively review project level clinical metrics with SGTMs to ensure compliance and accuracy of data. Support SGTMs during Project Review Meetings . Ensure compliance to all critical data fields within Project Management systems/ applicable trackers. Coach SGTMs on running and reviewing various project reports
• Resourcing and Talent planning of the SGTM team. Manage the team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance as well as project related trainings.
• Conduct progress reviews and evaluations in addition to create contingency plans to mitigate project, program-level and enterprise risks.
• Mentor SGTMs for further development and ensure they follow an Individual development plan.

Qualifications
• Bachelor's Degree Bachelor's Degree in life sciences or related field required Req
• Requires 10 years of clinical research experience including 6 years leadership experience, multi-regional and global focus or equivalent combination of education, training and experience.
• Requires broad management knowledge to lead cross-regional teams, and well as the ability to influence others outside of own job area regarding policies, procedures, and goals.
• Knowledge of clinical trials - In depth knowledge and skill in applying, applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Strong understanding of the Clinical Research Industry and the relevant environments in which it operates.;
• People Management - Proven ability to manage a team and work alongside others in a global environment to deliver results whilst meeting quality and timeline metrics. Provides others with a clear direction, delegates work appropriately and fairly, motivates and empowers others, monitors/manages performance and provides feedback and coaching, recruits, develops and retains staff of a high caliber. Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues
• Collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences. Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Leadership - Ability to successfully manage competing priorities. Excellent customer service skills and demonstrated ability to understand customer needs, have difficult conversations with internal stakeholders and customers as well as negotiate solutions. Good judgment and decision making skills.
• Organization - Strong presentation skills. Strong organizational and problem-solving skills. Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving. Strong understanding of other IQVIA functions and their inter-relationship with Project Support Units.
• Communication - Excellent communication skills, including good command of English language.
• Results Oriented - Demonstrated ability to deliver results to the appropriate quality and timeline metrics.
• IT Skills - Strong software and computer skills, including Microsoft Office applications.
• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, Innovation, Ownership).

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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